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Identifying HIPK1 as Target of miR-22-3p Enhancing Recombinant Protein Production From HEK 293 Cell by Using Microarray and HTP siRNA Screen
被引:11
作者:
Inwood, Sarah
[1
,2
]
Buehler, Eugen
[3
]
Betenbaugh, Michael
[2
]
Lal, Madhu
[3
]
Shiloach, Joseph
[1
]
机构:
[1] NIDDK, Biotechnol Core Lab, NIH, Bethesda, MD 20892 USA
[2] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[3] NIH, Chem Genom Ctr, Natl Ctr Adv Translat Sci, Rockville, MD 20850 USA
关键词:
microRNA;
siRNA;
miR-22-3p;
microarray;
HIPK1;
protein expression;
CHO-CELLS;
MAMMALIAN-CELLS;
BETA-CATENIN;
EXPRESSION;
FAMILY;
TRANSCRIPTION;
PREDICTION;
PATHWAY;
GROWTH;
PHOSPHORYLATION;
D O I:
10.1002/biot.201700342
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Protein expression from human embryonic kidney cells (HEK 293) is an important tool for structural and clinical studies. It is previously shown that microRNAs (small, noncoding RNAs) are effective means for improved protein expression from these cells, and by conducting a high-throughput screening of the human microRNA library, several microRNAs are identified as potential candidates for improving expression. From these, miR-22-3p is chosen for further study since it increased the expression of luciferase, two membrane proteins and a secreted fusion protein with minimal effect on the cells' growth and viability. Since each microRNA can interact with several gene targets, it is of interest to identify the repressed genes for understanding and exploring the improved expression mechanism for further implementation. Here, the authors describe a novel approach for identification of the target genes by integrating the differential gene expression analysis with information obtained from our previously conducted high-throughput siRNA screening. The identified genes were validated as being involved in improving luciferase expression by using siRNA and qRT-PCR. Repressing the target gene, HIPK1, is found to increase luciferase and GPC3 expression 3.3- and 2.2-fold, respectively.
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页数:9
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